{{Rsnum
|rsid = 28937899
|Gene = OPA3
|geno1 = (C;C)
|geno2 = (C;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=G
|Chromosome=19
|position=45553639
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OPA3
}}{{omim
| id = 606580
| variant = 0003
| desc    = OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT
| rsnum   = 28937899
}}
{{ neighbor
| rsid = 28937898
| distance = 36
}}

{{omim
|id=258501
|rsnum=28937899
}}

{{ClinVar
|rsid=28937899
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=46056897
|CHROM=19
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=OPA3:80207
|GENE_NAME=OPA3
|GENE_ID=80207
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.46056897G>A
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=258501
|CLNDBN=3-Methylglutaconic aciduria type 3
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000020909.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1473:C0574084:258501:67047:297232009
|CLNSRC=GeneReviews
|CLNSRCID=NBK1473
|Disease=3-Methylglutaconic aciduria type 3
}}

{{PMID Auto
|PMID=18985435
|Title=Costeff optic atrophy syndrome: new clinical case and novel molecular findings.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}